Androgen receptor modulatory miR-1271-5p can promote hormone sensitive prostate cancer cell growth

In most patients with advanced prostate cancer treated with hormonal therapy, androgen independence eventually emerges, leading to death. Androgen receptor signalling remains an important prostate cancer driver, even in the advanced disease stage. MicroRNAs (miRs), non-coding RNAs that regulate gene expression by inhibiting translation and/or promoting degradation of target mRNAs, can act as tumour suppressors or "oncomiRs" and modulate tumour growth. Because of their stability in tissues and in circulation, and their specificity, microRNAs have emerged as potential biomarkers, as well as therapeutic targets in cancer. We identified miR-1271-5p as an androgen receptor modulatory microRNA and we show it can promote hormone sensitive prostate cancer cell growth. Inhibition or overexpression of miR-1271-5p levels affects prostate cancer cell growth, apoptosis and expression of both androgen receptor target genes and other genes that are likely direct targets, dependent on androgen receptor status, and tumour stage. We conclude that miR-1271-5p has the potential to drive progression of hormone-dependent disease and that the use of specific inhibitors of miR-1271-5p may have therapeutic potential in prostate cancer.

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Publication Details

Journal
Frontiers in Oncology
Published
2024-08-29
DOI
https://doi.org/10.3389/fonc.2024.1440612
Primary Topic
Cancer-related molecular mechanisms research
Type
article
Field-Weighted Citation Impact
0.00

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article

Androgen receptor modulatory miR-1271-5p can promote hormone sensitive prostate cancer cell growth

Foteini Kalofonou, Charlotte L. Bevan, Damien A. Leach, Claire Fletcher et al.
Frontiers in Oncology
Cancer-related molecular mechanisms research
article

Androgen receptor modulatory miR-1271-5p can promote hormone sensitive prostate cancer cell growth

Foteini Kalofonou, Charlotte L. Bevan, Damien A. Leach, Claire Fletcher, Jonathan Waxman, Sue M. Powell
article en

Abstract

In most patients with advanced prostate cancer treated with hormonal therapy, androgen independence eventually emerges, leading to death. Androgen receptor signalling remains an important prostate cancer driver, even in the advanced disease stage. MicroRNAs (miRs), non-coding RNAs that regulate gene expression by inhibiting translation and/or promoting degradation of target mRNAs, can act as tumour suppressors or "oncomiRs" and modulate tumour growth. Because of their stability in tissues and in circulation, and their specificity, microRNAs have emerged as potential biomarkers, as well as therapeutic targets in cancer. We identified miR-1271-5p as an androgen receptor modulatory microRNA and we show it can promote hormone sensitive prostate cancer cell growth. Inhibition or overexpression of miR-1271-5p levels affects prostate cancer cell growth, apoptosis and expression of both androgen receptor target genes and other genes that are likely direct targets, dependent on androgen receptor status, and tumour stage. We conclude that miR-1271-5p has the potential to drive progression of hormone-dependent disease and that the use of specific inhibitors of miR-1271-5p may have therapeutic potential in prostate cancer.

Frontiers in OncologyVol. 14
Prostate Cancer Research (GB), Imperial College London (GB)
Cancer Research UK, National Institute for Health and Care Research, Imperial College London, Imperial College Healthcare NHS Trust, Prostate Cancer UK, A.G. Leventis Foundation
Good health and well-being
Openalex Percentile: Top 79%
Cancer-related molecular mechanisms research
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Androgen receptor modulatory miR-1271-5p can promote hormone sensitive prostate cancer cell growth — Foteini Kalofonou, Charlotte L. Bevan, et al. · Frontiers in Oncology (2024) | TGRS Research Map | TGRS